PE20081636A1 - ANTHRANILAMIDE INHIBITORS FOR AURORA KINASE - Google Patents

ANTHRANILAMIDE INHIBITORS FOR AURORA KINASE

Info

Publication number
PE20081636A1
PE20081636A1 PE2008000182A PE2008000182A PE20081636A1 PE 20081636 A1 PE20081636 A1 PE 20081636A1 PE 2008000182 A PE2008000182 A PE 2008000182A PE 2008000182 A PE2008000182 A PE 2008000182A PE 20081636 A1 PE20081636 A1 PE 20081636A1
Authority
PE
Peru
Prior art keywords
phenyl
amino
inhibitors
aurora kinase
pyrimidinyl
Prior art date
Application number
PE2008000182A
Other languages
Spanish (es)
Inventor
Jeffrey Michael Axten
Deborah L Bryan
David Harold Drewry
Thomas H Faitg
Timothy Francis Gallagher
Neil W Johnson
Jiri Kasparec
Jeffrey M Ralph
Domingos J Silva
Original Assignee
Smithkline Beecham Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=39644890&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20081636(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Smithkline Beecham Corp filed Critical Smithkline Beecham Corp
Publication of PE20081636A1 publication Critical patent/PE20081636A1/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/04—Antineoplastic agents specific for metastasis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
    • C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
    • C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D241/14—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D241/20—Nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

Abstract

SE REFIERE A COMPUESTOS DERIVADOS DE ANTRANILAMIDA DE FORMULA (I) DONDE R1 ES H, COOH, ALCOXI(C1-C6), CF3, ENTRE OTROS; R2 ES H, HALO, ALQUILO(C1-C3), CN, ENTRE OTROS; R3 ES H, FENILO, MORFOLINO-CH2CH2-FENILO, ENTRE OTROS; R4 ES HALO, ALQUILO(C1-C3) O ALCOXI(C1-C3); r ES DE 1 A 3; s ES DE 0 A 2. SON COMPUESTOS PREFERIDOS: 2-{[5-FLUORO-2-({3-[2-(4-MORFOLINIL)ETIL]FENIL}AMINO)-4-PIRIMIDINIL]AMINO}-N-(2-HIDROXIETIL)BENZAMIDA, (3R)-1-({2-[(5-FLUORO-2-{[3-(4-METIL-1-PIPERAZINIL)FENIL]AMINO}-4-PIRIMIDINIL)AMINO]FENIL}CARBONIL)-3-PIRROLIDINOL, (3R)-1-[(2-{[5-METIL-2-({3-[2-(4-MORFOLINIL)ETIL]FENIL}AMINO)-4-PIRIMIDINIL]AMINO}FENIL)CARBONIL]-3-PIRROLIDINOL, ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA AURORA QUINASA SIENDO UTILES EN EL TRATAMIENTO DE CANCERREFERS TO COMPOUNDS DERIVED FROM ANTRANYLAMIDE OF FORMULA (I) WHERE R1 IS H, COOH, ALCOXY (C1-C6), CF3, AMONG OTHERS; R2 IS H, HALO, (C1-C3) ALKYL, CN, AMONG OTHERS; R3 IS H, PHENYL, MORPHOLINO-CH2CH2-PHENYL, AMONG OTHERS; R4 IS HALO, (C1-C3) ALKYL OR (C1-C3) ALCOXY; r IS FROM 1 TO 3; s IS FROM 0 TO 2. PREFERRED COMPOUNDS ARE: 2 - {[5-FLUORO-2 - ({3- [2- (4-MORPHOLINYL) ETHYL] PHENYL} AMINO) -4-PYRIMIDINYL] AMINO} -N- ( 2-HYDROXYETHYL) BENZAMIDE, (3R) -1 - ({2 - [(5-FLUORO-2 - {[3- (4-METHYL-1-PIPERAZINYL) PHENYL] AMINO} -4-PYRIMIDINYL) AMINO] PHENYL} CARBONYL) -3-PYRROLIDINOL, (3R) -1 - [(2 - {[5-METHYL-2 - ({3- [2- (4-MORPHOLINYL) ETHYL] PHENYL} AMINO) -4-PYRIMIDINYL] AMINO} PHENYL) CARBONYL] -3-PYRROLIDINOL, AMONG OTHERS. IT ALSO REFERS TO A PHARMACEUTICAL COMPOSITION. SUCH COMPOUNDS ARE INHIBITORS OF AURORA KINASE, BEING USEFUL IN THE TREATMENT OF CANCER

PE2008000182A 2007-01-26 2008-01-24 ANTHRANILAMIDE INHIBITORS FOR AURORA KINASE PE20081636A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US88667607P 2007-01-26 2007-01-26

Publications (1)

Publication Number Publication Date
PE20081636A1 true PE20081636A1 (en) 2009-01-10

Family

ID=39644890

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2008000182A PE20081636A1 (en) 2007-01-26 2008-01-24 ANTHRANILAMIDE INHIBITORS FOR AURORA KINASE

Country Status (10)

Country Link
US (2) US7884098B2 (en)
EP (1) EP2121637A4 (en)
JP (1) JP5337712B2 (en)
AR (1) AR065015A1 (en)
AU (1) AU2008207809B2 (en)
CA (1) CA2676257A1 (en)
CL (1) CL2008000197A1 (en)
PE (1) PE20081636A1 (en)
TW (1) TW200902010A (en)
WO (1) WO2008092049A1 (en)

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CA2853498A1 (en) 2011-10-28 2013-05-02 Celgene Avilomics Research, Inc. Methods of treating a bruton's tyrosine kinase disease or disorder
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JP6469567B2 (en) 2012-05-05 2019-02-13 アリアド・ファーマシューティカルズ・インコーポレイテッド Compound for inhibiting cell proliferation of EGFR-activated cancer
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Also Published As

Publication number Publication date
CA2676257A1 (en) 2008-07-31
US7625903B2 (en) 2009-12-01
JP2010516780A (en) 2010-05-20
US20100016318A1 (en) 2010-01-21
CL2008000197A1 (en) 2008-08-01
EP2121637A4 (en) 2010-10-06
WO2008092049A1 (en) 2008-07-31
US7884098B2 (en) 2011-02-08
US20080182852A1 (en) 2008-07-31
AU2008207809B2 (en) 2013-04-18
JP5337712B2 (en) 2013-11-06
EP2121637A1 (en) 2009-11-25
AU2008207809A1 (en) 2008-07-31
TW200902010A (en) 2009-01-16
AR065015A1 (en) 2009-05-13

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